What is the dose of milrinone (phosphodiesterase 3 inhibitor) for neonates and pediatric patients?

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Milrinone Dosing in Neonates and Pediatric Patients

For neonates and pediatric patients with cardiac dysfunction, milrinone should be administered with a loading dose of 50 mcg/kg given over 10-60 minutes, followed by a continuous infusion of 0.25-0.75 mcg/kg/min, with dose adjustment based on renal function. 1, 2

Dosing Recommendations

Standard Dosing

  • Loading dose: 50 mcg/kg IV infused over 10-60 minutes
  • Maintenance infusion:
    • Minimum: 0.375 mcg/kg/min
    • Standard: 0.5 mcg/kg/min
    • Maximum: 0.75 mcg/kg/min

Dosing in Renal Impairment

Milrinone is primarily excreted unchanged in the urine, requiring dose adjustment in renal dysfunction:

Creatinine Clearance (mL/min/1.73m²) Infusion Rate (mcg/kg/min)
5 0.2
10 0.23
20 0.28
30 0.33
40 0.38
50 0.43

For patients with severe renal impairment (CrCl ≤30 mL/min/1.73m²), reduce loading dose to 25 mcg/kg and maintenance infusion to 0.25 mcg/kg/min 3.

Special Considerations for Neonates

Neonates and young infants may have immature renal function and altered pharmacokinetics. Recent research suggests:

  • Developmental changes in clearance must be considered in neonates 4
  • For neonates with acute kidney injury (AKI) following cardiac surgery, dose adjustment based on AKI stage is recommended 4
  • Target therapeutic concentration range: 100-300 ng/mL 3

Clinical Applications

Milrinone is indicated for:

  • Cardiogenic shock
  • Congestive heart failure
  • Post-cardiac surgery support
  • Septic shock with myocardial dysfunction

Administration Guidelines

  1. Preparation:

    • Dilute milrinone to a concentration of 200 mcg/mL using 0.45% NaCl, 0.9% NaCl, or 5% Dextrose
    • Use a calibrated electronic infusion device for administration
  2. Monitoring:

    • Continuous cardiovascular monitoring is essential
    • Monitor blood pressure, heart rate, cardiac output, and clinical signs of perfusion
    • Assess renal function regularly
    • Watch for adverse effects including hypotension, arrhythmias, and thrombocytopenia
  3. Titration:

    • Titrate dose based on hemodynamic response
    • Duration of therapy depends on patient responsiveness

Potential Adverse Effects

  • Hypotension (particularly with rapid loading dose)
  • Ventricular arrhythmias
  • Headache
  • Thrombocytopenia (less common than with amrinone)

Practical Considerations

  • Milrinone has both inotropic and vasodilatory effects (inodilator)
  • Unlike catecholamines, milrinone does not significantly increase myocardial oxygen consumption
  • In pediatric patients with septic shock, milrinone has been shown to increase cardiac index and decrease systemic vascular resistance 5
  • Avoid rapid administration of loading dose to prevent hypotension
  • Ensure adequate intravascular volume before initiating therapy

Common Pitfalls to Avoid

  1. Failure to adjust dose in renal dysfunction - Milrinone accumulation can lead to toxicity
  2. Inadequate monitoring - Continuous hemodynamic monitoring is essential
  3. Confusing with amrinone - Potential fatal complications if drugs or dosages are interchanged
  4. Rapid administration - Can cause significant hypotension
  5. Using in hypovolemic patients - Ensure adequate volume status before administration

Milrinone's hemodynamic effects typically begin within 5-15 minutes of loading dose administration, with peak effects seen at 1-2 hours. The drug's half-life is prolonged in renal dysfunction, necessitating careful dose adjustment in these patients.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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